P
US7524656B2ExpiredUtilityPatentIndex 71

Method for producing an L-amino acid by enhancing expression of the yggA gene in an Escherichia bacterium

Assignee: AJINOMOTO KKPriority: Dec 30, 1998Filed: Sep 13, 2007Granted: Apr 28, 2009
Est. expiryDec 30, 2018(expired)· nominal 20-yr term from priority
Inventors:LIVSHITS VITALIY ARKADIEVICHZAKATAEVA NATALIA PAVLOVNANAKANISHI KAZUOALESHIN VLADIMIR VENIAMINOVICHTROSHIN PETR VLADIMIROVICHTOKHMAKOVA IRINA LYVOVNA
C07K 14/195C12P 13/14C12P 13/24C12P 13/10C12P 13/08C12P 13/04C07K 14/245
71
PatentIndex Score
6
Cited by
56
References
6
Claims

Abstract

A bacterium belonging to the genus Escherichia which has an ability to produce an L-amino acid, wherein the ability to produce the L-amino acid is increased by increasing expression of the yggA gene is described. A method for producing the L-amino acid using the bacterium is also described.

Claims

exact text as granted — not AI-modified
1. A method for producing an L-amino acid selected from the group consisting of L-glutamic acid and L-arginine comprising:
 I) cultivating in a culture medium an  Escherichia  bacterium which has an ability to produce an L-amino acid selected from the group consisting of L-glutamic acid and L-arginine, wherein said ability to produce the L-amino acid is increased by increasing the expression of a protein comprising the amino acid sequence shown in SEQ ID NO: 16, wherein the expression is increased relative to the expression of said protein in a wild-type  Escherichia  bacterium by increasing the copy number of the DNA coding for said protein or by replacing the native promoter with a stronger promoter for expression of the DNA coding for said protein, and 
 II) recovering the L-amino acid from the medium. 
 
     
     
       2. The method according to  claim 1 , wherein said L-amino acid is L-glutamic acid. 
     
     
       3. The method according to  claim 1 , wherein said L-amino acid is L-arginine. 
     
     
       4. The method according to  claim 1 , wherein the copy number of the DNA coding for said protein in said bacterium is increased. 
     
     
       5. The method according to  claim 4 , wherein said DNA is located on a multicopy vector. 
     
     
       6. The method according to  claim 4 , wherein said DNA is located on a transposon.

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